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Clinical Program Leader/Program Manager Job
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| Employer Name: BiotechCrossing |
SpiderID: 2267887 |
| Location: Cambridge, Massachusetts |
Date Posted: 6/9/2008 |
| Wage: |
Category: Biotech |
| Job Code: 5355124 |
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Job Description:

Description: Will work on large, complex registration programs with a large number of sites and a significant number of patients. Will work with the program Medical Directors to provide input to the clinical development plan (CDP). Uses in-depth knowledge of cardiovascular therapeutic area, TA strategies and operational expertise to oversee the Clinical Development Team (CDT), takes a leadership role in the implementation/execution of the CDP, and participates in the development of clinical trial protocol concept in collaboration with the Clinical Development Team. Takes a broad, strategic leadership role in ensuring the successful development and execution of the Clinical Development Plans; utilizes operational expertise, knowledge of TA strategy and TA scientific input when planning program feasibility, developing strategies for country selections, CRO/ vendors use and evaluations and planning for contingencies. SALARY: Salary commensurate with experience BENEFITS: SALARY: Salary commensurate with experience STATUS: Full Time Company Profile:COMPANY PROFILE: About Biogen Idec: Transforming Discovery into Care With operations across the Americas, Europe, and Asia, Biogen Idec (NASDAQ:BIIB) is one of the world's leading biotechnology companies, creating new standards of care in oncology, neurology, and immunology. Every day, employees of Biogen Idec make a difference in people's lives, through pioneering research and development, manufacturing, and our worldwide commercial capabilities. Learn more at www.biogenidec.com/careers. Biogen Idec is proud to be an equal opportunity employer RUBIO/7671BR/IMDV Job Requirements: Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development; Excellent project management skills, including risk assessment and contingency planning. Also requires excellent leadership, communication, management and organizational skills, along with problem solving, conflict resolution, and team building skills. 5+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations; Must have experience in cardiovascular therapeutic area.
For more information, please click here To visit us at BiotechCrossing.
For further information, please visit us online at http://www.biotechcrossing.com
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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: BiotechCrossing |
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| City: Pasadena |
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| State: California |
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| Zip: 91101 |
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Web Site: http://www.biotechcrossing.com
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